US2622416A - Separation of low boiling gas mixtures - Google Patents
Separation of low boiling gas mixtures Download PDFInfo
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- US2622416A US2622416A US84315A US8431549A US2622416A US 2622416 A US2622416 A US 2622416A US 84315 A US84315 A US 84315A US 8431549 A US8431549 A US 8431549A US 2622416 A US2622416 A US 2622416A
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- cold
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- 239000000203 mixture Substances 0.000 title claims description 25
- 238000000926 separation method Methods 0.000 title description 15
- 238000009835 boiling Methods 0.000 title description 8
- 238000000034 method Methods 0.000 claims description 41
- 238000005057 refrigeration Methods 0.000 claims description 18
- 239000000470 constituent Substances 0.000 claims description 12
- 238000000746 purification Methods 0.000 claims description 12
- 238000004140 cleaning Methods 0.000 claims description 11
- 238000005194 fractionation Methods 0.000 claims description 10
- 238000001704 evaporation Methods 0.000 claims description 5
- 230000008020 evaporation Effects 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 239000007789 gas Substances 0.000 description 81
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 229910052757 nitrogen Inorganic materials 0.000 description 18
- 239000001301 oxygen Substances 0.000 description 16
- 229910052760 oxygen Inorganic materials 0.000 description 16
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 15
- 238000012986 modification Methods 0.000 description 10
- 230000004048 modification Effects 0.000 description 10
- 230000000694 effects Effects 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 238000012546 transfer Methods 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 238000003889 chemical engineering Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000009834 vaporization Methods 0.000 description 3
- 230000008016 vaporization Effects 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 230000001172 regenerating effect Effects 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000004887 air purification Methods 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000012771 pancakes Nutrition 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J5/00—Arrangements of cold exchangers or cold accumulators in separation or liquefaction plants
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2210/00—Processes characterised by the type or other details of the feed stream
- F25J2210/40—Air or oxygen enriched air, i.e. generally less than 30mol% of O2
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S62/00—Refrigeration
- Y10S62/902—Apparatus
- Y10S62/909—Regeneration
Definitions
- The'present invention relates to a process for separatihg gas 'rniittures containing constituents ofd-ifiere'nt" boilingpoints and to the removal from 'suc'h gas mixtures ofconstituents which ten o' 'solidify at the conditions-of the separation rocess; More particularlyjthe' invention” is camera-ed with the separation of air mm nit-re gen n oxv'genand involves prevent-m the entry seqiient fractionation into its principal components: Inth'e absence of special'provision for theifremova'L thesed'epositsof frozen water and cafrbondiox ide 'very rapidly plug'up the gas passages'a'ofth heat excha-ngers'which have, therefore; to be thawed outafterrelatively' shortoperatingfp'eriods evenif the gas'mixtures have been previously partially purified by suitable chemical treatments.
- the refrigeration" requirements of the process represent basically" the hea'tlea-k sent's a suh stantial' item of investment and operating cost because of its high pressure level and the need for separate chemical purification facilities for this stream, as by scrubbing with NaOl-l solution.
- CO2 cannot be removed easily fro-m high pressure air by chilling, since the air liquefies before the CO2 is deposited on the chilling surface.
- Various attempts have been made, therefore, to eliminate this stream, utilizing concepts and techniques which have developed durin the last five years.
- regenerator units designed with the inclusion of separate flow paths for recycle unbalance, the increased cost results from the limited cross-sectional area across 7 which the thermal effect of the unbalance flow can be made effective. It is necessary to design such regenerator units for large air separation plants in the form of a large number of chambersof limited diameter (e. g. one foot) arranged for parallel flow of the gas streams therethrough, whereas by constructing a regenerator unit using by-pass unbalance rather than recycle unbalance, the
- FIG. 2 and Figure 3 illustrate certain modifications of this system in which a portion of a cold product gas is used for chilling the by-pass unbalance stream.
- the present invention involves the diversion of a small portion of the main air supply as an unbalance stream bypassing the principal air chilling and purification means such as alternating regenerators and/or recuperators, chilling and purifying theunbalance stream to remove at least the prin-' cipal portion of its CO2 and H20 contents in equipment separate from the principal heat exchange means and at a pressure not substantially exceeding that of the main stream, and utilizing the heat removed from the unbalance air stream invention may utilize the low cost and demonstrated operability of conventional-type simple regenerative cold accumulators, while simultaneously eliminating external low temperature'refrigeration means and separate compression of the unbalance stream, and reducing the latter to the minimum flow necessary for successful operation of the principal air chilling and purification means. More specific features and advantages of the invention will appear hereinafter.
- The'air compressed in compressor 3 is preferably cooled to about 100 FQby indirect heat exchange with water which may take lace in an afte'r coolerforming apart of the compressor uni-t 3'in a manner known per se.
- the air leaving compressor unit 3 may then be further cooled to about +60 FL in a conventional forecooler 5" by'direct contact with a circulating stream of waterwhi'ch has been previously cooled to a temperature of about 50 to 60 preferably by direct-contact with the N2 product gas stream.
- A- major portion,say about 96-93 volumes, of the aircooled in'forecooler is then supplied through line 1 and chilled to about 275 F. byheat-exchange in the conventional-type simple alternating cold accumulators or regenerator units I0 or l2 with a total of 100 volumes or oxygen and nitrogen supplied to the regenerators inseparate streams from conventional double fractionation column 60, as wi l appear more clearly hereinafter.
- Regenerator pairs In and I2 are preferably of the so-called ribbbon packed type.
- the cold storage medium in these cold accumulators is normally made by winding corrugated aluminum strip (about 25 mm. wide and 0.5 mm. thick) into a coil in a manner similar to the winding of a movie reel.
- a series of these coils commonly'called pancakes are placed on top of each other in the accumulator vessel.
- Duplicate alternating accumulators of this type are used for heat exchange of incoming air with product nitrogen on the one hand and of incoming air with product oxygen on the other hand.
- the incoming air and the product N2 or 02 streams are switched from one to the other of a pair of accumulators at approximately 3 minute intervals.
- regenerator pairs l0 and I2 comprise, therefore; a relatively large regenerator pair H] for accumulating the cold of the nitrogen product stream and a relatively small regenerator pair t2 for accumulating the cold of the oxygen product stream-
- the feed air is divided between the air nitrogeni accumulators on the one hand and the air-oxygen accumulators on the other hand in proportionto the heat capacity of the two product streams. It will be observed that the total quantity of air supplied to regenerator units in and: 12 is smaller than the total quantity of returned pro'ductgases.
- This difierence in gas quantities represents the unbalance required for the successful operation of the regenerators with respect to complete revaporization, during the coldstoring' cycles, of the ice and CO2 snow deposited from the air during the air chilling cycles.
- Nitrogen is supplied to regenerator units i0 and 12'; through lines I and I6, respectively, and oxygen through lines 18 and 20, respectively.
- Th'e'remaining. small portion 'of the inlet air, amountingv to about 2.2-to" 4.2 volumes, which has-not been supplied to the regenerator units 10 and 12 maybe passed through 'lineto a cooling unit 21 wherein it may be cooled somewhat below the forecooling temperature,-say to about to'50 F., in indirect heat exchange with evaporating ammonia, if desired, to reduce the load on the subsequent water removal equipment.
- the condensed water maybe drawn off and the air having now a temperature of" about 40 F. may be passed through line 29 to a system of alternating air driers 30 and '32 which may contain a suitable water absorbent such as silica gel, alumina gel, charcoal etc..
- the 002 remaining water contents of-the unbalance ai'r'stream is deposited in alternating exchangers 35 and 3's by means of chilling in heat exchange with an equivalent quantity'of cold purified a-ir withdrawn fromthe main air stream leaving regenerators l0 and I2 through line 40 at a temperature of, say, about #275 F.
- a chilled clean air stream amount toabout 18 volumes is branched-off line 40-through line 42.
- An amount of about 2.2 to 4.2 volumes'of this air' (in general an amount substantially equal to the quantity of unbalance air stream) is supplied through 11118544 or to exchangers 35 or 31 to chill the air supplied thereto through line 33 to a temperature of -265 to -2'75 FL, at which temperature waterand CO2 are essentially completely deposited in these exchangers.
- a close approach of the air chilling temperature to the temperature of the air in line 42 may be made possible bythe provision of adequate exchanger surface. In general, the closer this approach the higher will be the degree of purification from CO2.
- the chilling cycles of exchangers 35 and 37' may be of considerable duration extending over about 3-5 hours or more without appreciable plugging of the unbalance airflow path or any marked decrease in heat transfer rate being experienced.
- exchanger 3-5 on a chilling cycle and exchanger 3'! on a cleaning (ice and CO2 vaporization) cycle
- the operation of these exchangers is as follows.
- the small portion of the clean, cold, main air stream supplied through lines 42 and 44 to exchanger 35 is warmed during the chilling cycle of exchanger '35 in heat exchange with the air supplied through line 33 to a temperature of about F.
- This warmed air stream leaves exchanger 35 through line 41.
- a small proportion of the air in line 41 corresponding in amount to the slight excess of air compressed in compressor 3 over air separated in column EiLthat is about 0.2 volume, is passed through line 49 to exchanger 31.
- Line 49 is provided with a throttle valve 48 by means of which the pressure may be reduced to substantially atmosphericpressure- On its
- This gas first passes through the clean passageways of exchanger 31, i. e. the passageways through which the clean air stream from line 42 rather than the unbalance air stream containing CO2 and residual Water Was passed during the chilling cycle. It is then inverted and passed back through the fouled passageways, i. e. the passageways in which the CO2 and residual ice of the unbalance air stream are deposited during the chilling cycle to be eventually vented through line to the atmosphere.
- the clean gas in line 49 is first chilled by the cold stored in exchanger 31 without depositing impurities, since it is itself clean, and is then warmed while passing in a reverse direction over fouled surface.
- the vaporizable deposits saturate the cleaning stream and are thus slowly removed from the exchanger surface.
- This type of flow is employed primarily in order to reduce the quantity of heat introduced into the exchanger 3'! in the process of cleaning; it is much more effective in this regard than for example directing the clean warm stream of cleaning air into the cold end of the exchanger.
- the rate of cleaning may be increased by supplying a small amount of heat corresponding to a temperature rise of about 5 to F.
- the major portion of this stream is passed through line 46 to be admixed with the remaining portion of cold purified air, amounting to about 14-16 volumes, which was withdrawn from line 40 through line 42 and not used for chilling and purifying the unbalance air.
- the chilled purified unbalance air stream exiting from ex' changer 35 via line 51 is also mixed with the other purified air streams from lines 46 and 55.
- the mixed stream in line 53 which may amount to about volumes and which may have a temperature of about 235 to 245 F.
- a high efiiciency turbine expander 59 such as described in the publications referred to above, wherein it is expanded to slightly above atmospheric pressure and supplied to the upper low pressure section of tower 60 through line 6
- the mixing of the water of the warm air-stream from line 4-6 with the cold air streams from lines 56 and 51 in the manner described results in an increase in the temperature of the air entering expanders 59, to a level such that liquefaction of any significant amount of the gas stream during expansion is avoided. This is desired because of the loss in efficiency resulting from liquefaction taking place during expansion.
- the efiiciency of expanders 59 should be high, say about 80%, and the quantity of gas passed to the expanders should be so controlled that the refrigeration required by system is provided thereby. For example, by expanding approximately 20% of the process air from an initial condition of -236 F. and 6 atms. pressure to a final pressure of 1.35 atms. with 80% adiabatic efficiency, a refrigeration effect amounting to about 2.7 B. t. u./lb. of air processed is obtained. This is suificient to provide the refrigeration requirement of the process when operated on a large scale.
- the expanders operate at a discharge pressure corresponding to the pressure level of the low pressure section 63 of tower 60 so that the expanded gases in line 6
- double fractionation tower 60 comprising a low pressure secion 63, a high pressure section 65 and auxiliary heat exchange equipment is conventional throughout and need not be described in full detail for the purpose of the present invention. Briefly it may be stated that the tower 60 effects fractionation without the introduction of external heating or cooling.
- the elevated pressure of, say about 60-80 lbs. per sq. in. gauge under which high pressure section 65-may be operated raises the boiling points of the components of the air supplied through line 4
- Reboiler heat transfer in exchanger 61 is limited to the quantity required to condense all the air introduced through line 41.
- a relatively small number of plates in section 65 is sufiicient to effect separation into a pure liquid N2 stream withdrawn through line 69 to be employed for top reflux in the top of section 63 and an oxygen enriched bottoms fraction withdrawn through line H to be used as the liquid feed stream for section 63.
- the latter stream may be passed through porous filters T3 to remove solid CO2 entrained from the regenerators before it is vented into section 63. It may also pass through a bed of silica gel 14 employed to reduce the quantity of acetylene or other light hydrocarbons introduced into the tower. Filter l3 and bed 74 may be regenerated at intervals.
- Both the liquid bottoms fraction and the liquid N2 withdrawn from section 65 through line 69 are preferably subcooled in heat exchangers BI and 11 by heat exchange with gaseous product N2 withdrawn through line 19 from the top of tower section 63 to reduce vaporization loss on throttling.
- the nitrogen stream in line 69 is vented into the top of column section 63 as previously described to provide the necessary reflux.
- Column section 63 preferably operates under a pressure of about 3 to 8 p. s. i. gauge, only sufficient to overcome friction losses inthe product discharge lines.
- the oxygen-containing feed streams to tower section 63 comprise the liquid oxygen-enriched bottoms product of tower section 65 and the cold gaseous air leaving theexpander 59 through line 6
- the amount of reflux available is generally barely sufficient to effect the separation of these streams into oxygen and nitrogen of fairly high purity so that a relatively large number of plates operating with high efficiency is normally required.
- argon is also present in air as a third component, special means for argon removal may be provided if both'the oxygen and nitrogen products must be of very high purity. This is not contemplated in the example here described, where an oxygen purity of about is satisfactory.
- the Nz taken through line 19 as an overhead gaseous product is employed to subcool the reflux N2 in line 69 by means of heat exchanger 1! and is then passed preferably to further heat exchange with the liquid feed stream to tower B3 in heat All or a portion; of the N2 leaving regeneratorsfl through line 85 may finally be employed tocool the water used: in. air ...f01.8?COO19r- 5.
- Gaseous product oxygen is withdrawn :from the bot-tom of tower sectionifilithrough'.line178. It- -may be adjusted. :in temperature by: passage it'hroughsexchanger :82 before. entering .regenerator :un its I 2 as. previously :described to cool :and :purify.”-the incoming. air.- .Product 02 'iswithdrawn-through line 86.
- a fractional percentage of nitrogen fouled by use as a cleansing'ga's in this way is bled 'off through line 5 I ,and a substantially'larger stream of nitrogen warmed by the' exchangeof heat in chilling and purifying the .by-passair streamis' withdrawnthrough line I 46.
- Another possible modification within thespirit of the invention involves the'feed'ofall 'of the chilled and purified air boththe mainstream and the unbalance stream to" the bottom ofthe high pressure tower section, and the withdrawal from 'the top'of this tower section-of a -gaseous stream of Nz'at'the eleveated tower pressure'of about -80 p. s. i. gauge. This stream may amount'to about'2'0 volume percent-on the air feed. A portion of-this cold'Nz stream-may'then be used to chill and purify the unbalance'air stream in themanner previously described.
- the high pressure nitrogen stream 246 is warmed in the same manner as N2 stream 146 in Figure 2 or air stream-46 in Figure 1, bypheat exchange with the by-pass air stream in "condensers 35 and 31.” Here, however; it iscombined with and pre warmsthe remaining portion ofthe cold high-pressure'nitrogen from line 261, .in'line 256.
- the prewarmed nitrogen stream'in'line255, work expanded in expander 259, is rechil'led thereby and passes through line 2Bl to"line 19' leaving the top of the low pressure'section 63 of i the fractionating' tower.
- Thecooling effect of the workexpansion step is thus availablefor heat exchange-in exchangers '11 and 8i,- in sub' stantially the same manner as in the modification shown in Figure 1.
- the method of separating gas mixtures by liquefaction and fractionation which comprises charging the major proportion of a gas mixture to be separated at a super-atmospheric pressure to chilling and purification means to produce cold clean gas, chilling and purifying a minor proportion of said gas mixture in equipment separate from said means at substantially said super-atmospheric pressure so as to cool said minor proportion and remove at least the major proportion of its solidifying constituents, said separate equipment comprising heat exchange means operating by the recuperative principle in chilling cycles and cycles serving the evaporation of solidified gas mixture constituents deposited in said recuperative means, passing a minor proportion of said first named cold clean gas through said recuperative means during their chilling cycle to warm said minor proportion of cold clean gas, passing a minor proportion of said clean gas so warmed through said recuperative means during said cleaning cycle to remove said deposits, mixing the remaining portion of said warmed clean gas with a second minor proportion of said first named cold clean gas, subjecting the mixture so obtained to work expansion to provide refrigeration and utilizing said refrigeration in said process.
- the method of separating a gas mixture by liquefaction and fractionation which comprises charging the major portion of the gas mixture at a superatmospheric pressure to chillingand purification means to produce a first stream of cold clean gas by means of heat exchange with separate streams of cold clean gas representing separated product constituents the total quantity of which is larger than the quantity of said major portion of the gas mixture, chilling and purifying the remaining minor portion of said gas mixture at substantially said superatmospheric pressure in equipment separate from said means so as to 0001 said minor portion and remove at least the major part of its solidifying constituents, said separate equipment comprising heat exchange means operating by the recuperative principle in chilling cycles and cycles serving the evaporation of solidified gas constituents deposited therein, passing through said recuperative means during their chilling cycle a relatively small amount of a second clean gas stream derived from one of said streams of cold clean gas to warm said second clean gas stream, passing a minor portion of said second clean gas so warmed through said recuperative means during their cleaning cycle to remove the deposits therefrom, transferring heat absorbed
- said second cold clean gas stream is a portion of a coldseparated main gas constituent
- said third cold clean gas stream is a chilled portion of said gas mixture
- said heat transfer is effected by the indirect exchange of heat between said third stream andat least part of the warmed portion of said second stream.
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Description
Dec. 23, 1952 H. J. osoRzALY SEPARATION OF LOW BOILING GAS MIXTURES Filed March 50, 1949 5 Sheets-Sheet l Wa M Attorney all l Dec. 23, 1952 H. J; OGORZALY SEPARATION OF LOW BOILING GAS MIXTURES 3 Sheets-Sheet 2 wuobq wmzu w wb WE -24 .I
Filed March 30, 1949 All m mobqmmzmwuu C by tra'n'sfer to the' product streams.
Patented Dec. 23, 1952 UNITED STAT ES PATENT or rice sEPARATIoNi i;% n0IL1NG GAS Henrv'J. Ogo'rzaly; S'ummit,.'N; J., assignorto Standard Oil Development Company,-. a eorpo ration of Delaware Application March- 30, 1949;""SeriaYNo. 845315 The'present invention "relates to a process for separatihg gas 'rniittures containing constituents ofd-ifiere'nt" boilingpoints and to the removal from 'suc'h gas mixtures ofconstituents which ten o' 'solidify at the conditions-of the separation rocess; More particularlyjthe' invention" is camera-ed with the separation of air mm nit-re gen n oxv'genand involves prevent-m the entry seqiient fractionation into its principal components: Inth'e absence of special'provision for theifremova'L thesed'epositsof frozen water and cafrbondiox ide 'very rapidly plug'up the gas passages'a'ofth heat excha-ngers'which have, therefore; to be thawed outafterrelatively' shortoperatingfp'eriods evenif the gas'mixtures have been previously partially purified by suitable chemical treatments. The" accumulation of such deposits maybe preventedby the use of heat exchange equi inent-eniployingan alternation or flow paths to. fi'c't'thel cooling ofthe inlet gas; in a manner well known in the art of 'air separation. For this plir'po's'ejswitchi'ng regenerators' have been used whiclrare. kept in operating condition by the periodic revaporizationof deposited ice and CO;v
snow into low pressure streams ofoxygen and nitrogenproduced inthe. process itself. and passed during-thecold storage cycle; through the passages: ofr the regenerators: through which, in a previously air cooling cyc1e,-the air hasbeen passed. depositingrits water and CO2 in solid'form; In this-manner, the ice:' and: solid 002* evaporate into'-the low' press'urepro'ductstreams while simultaneously-the heat-absorbed the regenerators': during? the chilling of theair to operating temperatures in": the previous cycle 'is" removed Recupera e heat exchangersmaybe used in a sim'ier'. s
002* into" the" separation means by" 'r-to permit the" removalof "ice and solid' alternating regenerators in--themariner "indicated; the mass or Ywi'ght qf -iow ressure" product ga'swhich is passed over "the 14 claims.- 01. 62-'175.5)
surface supporting the deposited ice and CO2 mus-t; lee-greater than themass of air from the ice and 002 tobe removed was previously deposited. The reason for this requirement is the factthat the low pressure gas has a smaller heat capacity per unit mass than the air introduced at arelatively high pressure; With equal flow quantities of lowpressure product gases and-high pressure air, this difference in heat capacity results in excessive temperature differentials in the colder parts of the apparatus which prevent the successful removal of the deposited ice and 602; I The-required difference between the quantity ofair from which the solid impurities aredeposited and the quantity of low pressure gas-required for "the removal of these deposits is gene raily calledthe mass unbalance of the systemr This'phenomenon is'well known in the art"(see for instance Air Purification in the Reversi'ng Exchanger, W. E. Lobo et al.,-Chemical Engineering Progress, vol. 43, No. 2, pages 69-73, February 1947). Various methods have been proposed and used heretofore toacccmplish this unbalance and with item efficient operation of theregenerators'br other types of heat exchangers for chilling the incoming air to fractionation temperatures and effecting its-purification; Iti's" of importance that the methodem- 307-} ployed be such as will permit efficient' separation ofthe"chi1led' air in subsequent fractionatin'g equipment, with high recovery of theoxygen compdnentfin relatively'pui'e' form.
Oneof themethods known to the priorart' involve's'by pas'sihg a small proportion (ofthe order of 2-676) of' the inlet air stream around" the regenerators in order to achieve the unbalance,- chemically puriiying this side stre'anito remove COaexpahdiing through a work-engin lastream of gaseous Nz withdrawnf-rom'the top' ofthehighpressure (5-6 atmsi) feed tower of the conventional double tower fractionation sys tem, to developsome of the-necessary refrigeration, and introducing additional refrigeration through-the small air stream which by-passes the'regenerators; by' means of a very high; levelofcompression(-200 atms.) and through auxiliaryrefrigeration-of this streamwith evaporating'l'ammonia. The refrigeration" requirements of the process represent basically" the hea'tlea-k sent's a suh stantial' item of investment and operating cost because of its high pressure level and the need for separate chemical purification facilities for this stream, as by scrubbing with NaOl-l solution. CO2 cannot be removed easily fro-m high pressure air by chilling, since the air liquefies before the CO2 is deposited on the chilling surface. Various attempts have been made, therefore, to eliminate this stream, utilizing concepts and techniques which have developed durin the last five years.
In general, the trend of these efforts has been toward the development of a completely low pressure (i. e., 5-7 atms.) process, in which the unbalance required for satisfactory vaporization of the CO2 deposited on chilling the incoming air is obtained not by the expedient of by-passing a small portion of the entering air around the chillin and purification means, but rather by recycling 2, small cold gas stream through the chilling means through a path which is physically separated from but in thermal contact with the paths of the inlet air and product gas streams. The by-pass air stream is thus completely eliminated, the air previously introduced in this manner being included in the main air stream entering the process.
The prospects of accomplishing such a completely low pressure process have been considerably improved by the recent development of more efficient gas expansion turbines and of process flow schemes allowing the expansion of a larger quantity of gas than has been the case in previous operations. This permits the generation of the necessary refrigeration for the process entirely by means of the Work-expansion of a process gas stream, and it is no longer necessary to compress a small portion of the incoming air to high pressure levels and to provide for auxiliary refrigeration and chemical purification of this stream. Systems of this type are discussed in Chemical Engineering Progress vol. 43, No. 1, pages 21- 26 (January, 1947) and vol. 43, No. 2, pages 61- 90 (February, 1947).
While the use of low pressures throughout is a desirable development both technically and economically, the provision of a separate flow path for internally recycling unbalance gas, which is thermally bonded to the flow path for the incoming air stream, is not completely satisfactory from an economic viewpoint. It is this feature which permits the elimination of the requirement for introducing a small portion of the inlet air through a separate flow path whivh bypasses the regenerators and therefore requires separate purification and chilling facilities. The scheme of unbalancing by recycle of cold gas through a separate fiow path which is thermally bonded to the main flow path may be applied to heat exchange means using either the regenrative or the recuperative scheme of heat transfer, but in allcases a very substantial increase in cost of the principal heat exchange means relative tosimple regenerators is encountered.
In the case of regenerators designed with the inclusion of separate flow paths for recycle unbalance, the increased cost results from the limited cross-sectional area across 7 which the thermal effect of the unbalance flow can be made effective. It is necessary to design such regenerator units for large air separation plants in the form of a large number of chambersof limited diameter (e. g. one foot) arranged for parallel flow of the gas streams therethrough, whereas by constructing a regenerator unit using by-pass unbalance rather than recycle unbalance, the
' characteristicof the conventional simple regenerators, and costs of fabricating such exchangers are high in relation to the conventional simple regenerators.
Accordingly it appears that the lowest investment cost for a large scale oxygen plant will be obtained by a combination process utilizing conventional-type simple regenerators with air bypass unbalance, combined with a process flow which will enable the by-pass air stream to be introduced at the pressure of the main air stream or at a lower pressure. The present invention is directed to a combination process of this type which avoids the difficulties outlined above and which affords various additional advantagesas will be apparent from the subsequent detailed description wherein reference will be made to the;
accompanyin drawings, in which Figure 1 illustrates schematically a system suit able to carry out a preferred embodiment of the invention; and
Figure 2 and Figure 3 illustrate certain modifications of this system in which a portion of a cold product gas is used for chilling the by-pass unbalance stream.
Broadly speaking, the present invention involves the diversion of a small portion of the main air supply as an unbalance stream bypassing the principal air chilling and purification means such as alternating regenerators and/or recuperators, chilling and purifying theunbalance stream to remove at least the prin-' cipal portion of its CO2 and H20 contents in equipment separate from the principal heat exchange means and at a pressure not substantially exceeding that of the main stream, and utilizing the heat removed from the unbalance air stream invention may utilize the low cost and demonstrated operability of conventional-type simple regenerative cold accumulators, while simultaneously eliminating external low temperature'refrigeration means and separate compression of the unbalance stream, and reducing the latter to the minimum flow necessary for successful operation of the principal air chilling and purification means. More specific features and advantages of the invention will appear hereinafter.
Referring now to the drawings, the system illustrated therein will be described first as to Figure 1 using as an example the separation of unit volumes of air into oxygen and nitrogen. Anamount of slightly more than 100 unit'volumes, say about 100.2 unit volumes, of air is supplied through line I to compressor 3 wherein it may be compressed to a moderate pressure of the order of 5-7 atms. abs. For reasons of simplicity there has not been included at this point the small quantity of additional air which must be' supplied at" the same pressure level to make up forthe losses which are experienced when a conventional-type simple cold accumulator or regenerator filled with air under pressure is switched to connect with the product gas lines, at which time at least a portion of the air under pressure in the regenerator is generally vented to the'atmosphere. The air required to makeup for these-losses may amount to an additional 3 1 .61%
I The'air compressed in compressor 3 is preferably cooled to about 100 FQby indirect heat exchange with water which may take lace in an afte'r coolerforming apart of the compressor uni-t 3'in a manner known per se. The air leaving compressor unit 3 may then be further cooled to about +60 FL in a conventional forecooler 5" by'direct contact with a circulating stream of waterwhi'ch has been previously cooled to a temperature of about 50 to 60 preferably by direct-contact with the N2 product gas stream. This step-reduces the load on the main heat'exchange equipment comprising conventional regenerator units and I2 and also provides for a steadier operation of these regenerators by substantially reducing the water content of the entering air.
A- major portion,say about 96-93 volumes, of the aircooled in'forecooler is then supplied through line 1 and chilled to about 275 F. byheat-exchange in the conventional-type simple alternating cold accumulators or regenerator units I0 or l2 with a total of 100 volumes or oxygen and nitrogen supplied to the regenerators inseparate streams from conventional double fractionation column 60, as wi l appear more clearly hereinafter. Regenerator pairs In and I2 are preferably of the so-called ribbbon packed type. The cold storage medium in these cold accumulators is normally made by winding corrugated aluminum strip (about 25 mm. wide and 0.5 mm. thick) into a coil in a manner similar to the winding of a movie reel. A series of these coils commonly'called pancakes are placed on top of each other in the accumulator vessel. Duplicate alternating accumulators of this type are used for heat exchange of incoming air with product nitrogen on the one hand and of incoming air with product oxygen on the other hand. The incoming air and the product N2 or 02 streams are switched from one to the other of a pair of accumulators at approximately 3 minute intervals.
-The regenerator pairs l0 and I2 comprise, therefore; a relatively large regenerator pair H] for accumulating the cold of the nitrogen product stream and a relatively small regenerator pair t2 for accumulating the cold of the oxygen product stream- The feed air is divided between the air nitrogeni accumulators on the one hand and the air-oxygen accumulators on the other hand in proportionto the heat capacity of the two product streams. It will be observed that the total quantity of air supplied to regenerator units in and: 12 is smaller than the total quantity of returned pro'ductgases. This difierence in gas quantities represents the unbalance required for the successful operation of the regenerators with respect to complete revaporization, during the coldstoring' cycles, of the ice and CO2 snow deposited from the air during the air chilling cycles. Nitrogen is supplied to regenerator units i0 and 12'; through lines I and I6, respectively, and oxygen through lines 18 and 20, respectively.
Th'e'remaining. small portion 'of the inlet air, amountingv to about 2.2-to" 4.2 volumes, which has-not been supplied to the regenerator units 10 and 12 maybe passed through 'lineto a cooling unit 21 wherein it may be cooled somewhat below the forecooling temperature,-say to about to'50 F., in indirect heat exchange with evaporating ammonia, if desired, to reduce the load on the subsequent water removal equipment. The condensed water maybe drawn off and the air having now a temperature of" about 40 F. may be passed through line 29 to a system of alternating air driers 30 and '32 which may contain a suitable water absorbent such as silica gel, alumina gel, charcoal etc..
The bulk of the water vapor remaining' in the air stream is removed in" driers 3D-or 32- leaving type for a removal of the CO2 and residualwater contents of this air sidestream in the following manner.
The 002 remaining water contents of-the unbalance ai'r'stream is deposited in alternating exchangers 35 and 3's by means of chilling in heat exchange with an equivalent quantity'of cold purified a-ir withdrawn fromthe main air stream leaving regenerators l0 and I2 through line 40 at a temperature of, say, about #275 F. A chilled clean air stream amount toabout 18 volumes is branched-off line 40-through line 42. An amount of about 2.2 to 4.2 volumes'of this air' (in general an amount substantially equal to the quantity of unbalance air stream) is supplied through 11118544 or to exchangers 35 or 31 to chill the air supplied thereto through line 33 to a temperature of -265 to -2'75 FL, at which temperature waterand CO2 are essentially completely deposited in these exchangers. A close approach of the air chilling temperature to the temperature of the air in line 42 may be made possible bythe provision of adequate exchanger surface. In general, the closer this approach the higher will be the degree of purification from CO2. If the unbalance by-pass air stream'in line 33 has been freed of the bulk of its water content in absorbers 30 or 32, the chilling cycles of exchangers 35 and 37' may be of considerable duration extending over about 3-5 hours or more without appreciable plugging of the unbalance airflow path or any marked decrease in heat transfer rate being experienced.
Assuming exchanger 3-5 on a chilling cycle and exchanger 3'! on a cleaning (ice and CO2 vaporization) cycle, the operation of these exchangers is as follows. The small portion of the clean, cold, main air stream supplied through lines 42 and 44 to exchanger 35 is warmed during the chilling cycle of exchanger '35 in heat exchange with the air supplied through line 33 to a temperature of about F. This warmed air stream leaves exchanger 35 through line 41. A small proportion of the air in line 41 corresponding in amount to the slight excess of air compressed in compressor 3 over air separated in column EiLthat is about 0.2 volume, is passed through line 49 to exchanger 31. Line 49 is provided with a throttle valve 48 by means of which the pressure may be reduced to substantially atmosphericpressure- On its The unbalance air stream is then passed way through exchanger 31 this gas first passes through the clean passageways of exchanger 31, i. e. the passageways through which the clean air stream from line 42 rather than the unbalance air stream containing CO2 and residual Water Was passed during the chilling cycle. It is then inverted and passed back through the fouled passageways, i. e. the passageways in which the CO2 and residual ice of the unbalance air stream are deposited during the chilling cycle to be eventually vented through line to the atmosphere. By this procedure the clean gas in line 49 is first chilled by the cold stored in exchanger 31 without depositing impurities, since it is itself clean, and is then warmed while passing in a reverse direction over fouled surface. The vaporizable deposits saturate the cleaning stream and are thus slowly removed from the exchanger surface. This type of flow is employed primarily in order to reduce the quantity of heat introduced into the exchanger 3'! in the process of cleaning; it is much more effective in this regard than for example directing the clean warm stream of cleaning air into the cold end of the exchanger. The rate of cleaning may be increased by supplying a small amount of heat corresponding to a temperature rise of about 5 to F. prior to inverting the cleaning air stream by means of a heater 53 or by by-passing a small part of the warm cleaning air stream from line 49 around exchanger 3! to the opposite cold end, therebyv raising slightly the temperature of the stream entering the fouled passageway. This procedure may be desirable in many cases in spite of the somewhat increased refrigeration load resulting therefrom.
Returning now to the warmed clean air stream in line 41, the major portion of this stream, say about 2-4 volumes, is passed through line 46 to be admixed with the remaining portion of cold purified air, amounting to about 14-16 volumes, which was withdrawn from line 40 through line 42 and not used for chilling and purifying the unbalance air. The chilled purified unbalance air stream exiting from ex' changer 35 via line 51 is also mixed with the other purified air streams from lines 46 and 55. The mixed stream in line 53 which may amount to about volumes and which may have a temperature of about 235 to 245 F. is directed to a high efiiciency turbine expander 59, such as described in the publications referred to above, wherein it is expanded to slightly above atmospheric pressure and supplied to the upper low pressure section of tower 60 through line 6| at a temperature of about -300 F. The mixing of the water of the warm air-stream from line 4-6 with the cold air streams from lines 56 and 51 in the manner described results in an increase in the temperature of the air entering expanders 59, to a level such that liquefaction of any significant amount of the gas stream during expansion is avoided. This is desired because of the loss in efficiency resulting from liquefaction taking place during expansion. The efiiciency of expanders 59 should be high, say about 80%, and the quantity of gas passed to the expanders should be so controlled that the refrigeration required by system is provided thereby. For example, by expanding approximately 20% of the process air from an initial condition of -236 F. and 6 atms. pressure to a final pressure of 1.35 atms. with 80% adiabatic efficiency, a refrigeration effect amounting to about 2.7 B. t. u./lb. of air processed is obtained. This is suificient to provide the refrigeration requirement of the process when operated on a large scale. The expanders operate at a discharge pressure corresponding to the pressure level of the low pressure section 63 of tower 60 so that the expanded gases in line 6| may vent directly into that section where they undergo fractionation.
The operation of double fractionation tower 60 comprising a low pressure secion 63, a high pressure section 65 and auxiliary heat exchange equipment is conventional throughout and need not be described in full detail for the purpose of the present invention. Briefly it may be stated that the tower 60 effects fractionation without the introduction of external heating or cooling. The elevated pressure of, say about 60-80 lbs. per sq. in. gauge under which high pressure section 65-may be operated raises the boiling points of the components of the air supplied through line 4| to the bottom of section 65 to a level such that the heat of the N2 condensing in the top of section 65 may be used to reboil liquid 02 in the bottom of low pressure section 63. Reboiler heat transfer in exchanger 61 is limited to the quantity required to condense all the air introduced through line 41. A relatively small number of plates in section 65 is sufiicient to effect separation into a pure liquid N2 stream withdrawn through line 69 to be employed for top reflux in the top of section 63 and an oxygen enriched bottoms fraction withdrawn through line H to be used as the liquid feed stream for section 63. The latter stream may be passed through porous filters T3 to remove solid CO2 entrained from the regenerators before it is vented into section 63. It may also pass through a bed of silica gel 14 employed to reduce the quantity of acetylene or other light hydrocarbons introduced into the tower. Filter l3 and bed 74 may be regenerated at intervals. Both the liquid bottoms fraction and the liquid N2 withdrawn from section 65 through line 69 are preferably subcooled in heat exchangers BI and 11 by heat exchange with gaseous product N2 withdrawn through line 19 from the top of tower section 63 to reduce vaporization loss on throttling. The nitrogen stream in line 69 is vented into the top of column section 63 as previously described to provide the necessary reflux.
Column section 63 preferably operates under a pressure of about 3 to 8 p. s. i. gauge, only sufficient to overcome friction losses inthe product discharge lines. The oxygen-containing feed streams to tower section 63 comprise the liquid oxygen-enriched bottoms product of tower section 65 and the cold gaseous air leaving theexpander 59 through line 6|. The amount of reflux available is generally barely sufficient to effect the separation of these streams into oxygen and nitrogen of fairly high purity so that a relatively large number of plates operating with high efficiency is normally required. Since argon is also present in air as a third component, special means for argon removal may be provided if both'the oxygen and nitrogen products must be of very high purity. This is not contemplated in the example here described, where an oxygen purity of about is satisfactory. The Nz taken through line 19 as an overhead gaseous product is employed to subcool the reflux N2 in line 69 by means of heat exchanger 1! and is then passed preferably to further heat exchange with the liquid feed stream to tower B3 in heat All or a portion; of the N2 leaving regeneratorsfl through line 85 may finally be employed tocool the water used: in. air ...f01.8?COO19r- 5. Gaseous product: oxygen is withdrawn :from the bot-tom of tower sectionifilithrough'.line178. It- -may be adjusted. :in temperature by: passage it'hroughsexchanger :82 before. entering .regenerator :un its I 2 as. previously :described to cool :and :purify."-the incoming. air.- .Product 02 'iswithdrawn-through line 86.
The foregoing .zdescription' .has referred to a specific. method for achieving-an entirely-low pressure .process for air separation: employing mass'unbalancento permit longecontinuedz-operation .3 of alternating regenerative-type: equipment used has the principal air chilling andpu'rifyi'ng means, in which the. small I stream. or "air "bypassed around. the principal 1 air chilling; means to; effect the desired mass unbalance is :chilled and purifiedrin separate chilling means, and-in which the heat 1 abstracted from the streamot unbalance air is employed to-preheat a-:portion of vpurifiediair which is expanded in a work engine :toprovide. the refrigeration necessary for theprocess and then fractionated for the production of a stream comprisingprincipally"oxygen; Certain modifications of the procedure disclosed are: self-evident and it is not intended to disclaim .such modifications. For example, instead of employing a portion 'of the main air stream to chill the unbalance stream; a portion of the product 1% stream leaving the low pressure tower may equallywell be employed: for-the same purpose. The heat transferred to the-Na stream may'then be transferred in separate--heat exchange means to the air'stream passingtdthe expander witha total result "similar-to tha-t obtained in the procedure specificallydescribed. An advantage maybe gained in this-manner in that the by-pass stream may be cooledto a lower temperature and hence may "be more. completely purified.
'A-n operation of this type is illustrated in the attached Figure 2. This drawing-includes apartial-showing of the heat exchange-and fractionating equipment ofFigure 1 in which similar parts are similarly numbered and a difierent manifolding system is shown. Accordingto this modification of theinvention, a portionof the main-air stream 40, derived from the' r'egenerators m and 'IZ ofFigure his: withdrawn as aside stream -throughline 142 and used for worle existhus nitrogen instead of air, and the connecti'on-of-line 42 to line 44 in Figure l is eliminated.
.The internal manifolding andoperating-cycle for this exchanger system, for alternately cleansing the surface of one exchanger while-theother is on stream in the chilling-purifying stage-'of-the cycle, are otherwise quite similar 'to those 'in Figure 1.
A fractional percentage of nitrogen fouled by use as a cleansing'ga's in this way is bled 'off through line 5 I ,and a substantially'larger stream of nitrogen warmed by the' exchangeof heat in chilling and purifying the .by-passair streamis' withdrawnthrough line I 46.
10 The chilled and purified air from the 'by-pass stream, withdrawn throughlinevfi'l, iscombined with the :portionv of the main cold.v air stream withdrawn'athroughtiine L42 Beforespassing this combined'stream to the workexpander '59, however, it is prewarmed by indirect heat exchange in heat.:exchanger l5fl withthe warmnitrogen streamhin. line-1'46. The nitrogen streamxthus recooled is-returnedtoline 19 by way of line 141. The rprewarmedoairstreaml56, derived from lines= l42 .and' I5], is then. chilled by worker:- pension .in expander 59 and :passedthroughline fillin'to the middle portion'ofithelow pressure section 63 of fractionating tower 6'0. The-functionoi the regenerators and 'fractionating towers is otherwise essentially the same inthis modification 'of the -inventionas in'that illustratedin Figure 1.
Another possible modification within thespirit of the invention involves the'feed'ofall 'of the chilled and purified air boththe mainstream and the unbalance stream to" the bottom ofthe high pressure tower section, and the withdrawal from 'the top'of this tower section-of a -gaseous stream of Nz'at'the eleveated tower pressure'of about -80 p. s. i. gauge. This stream may amount'to about'2'0 volume percent-on the air feed. A portion of-this cold'Nz stream-may'then be used to chill and purify the unbalance'air stream in themanner previously described. "Ihe heated portion of this N2 streamv may then be mixed with the remaining cold gaseousNz' to provide a prewarrned Nzstreamunderpressure for expansion in the work engine to generate the refrigeration l-oad'oi'the process. The expanded N2 may be dischargedin'admixture with the'low pressure gaseous product N2 leaving the topof the low pressure tower I section. This modification of the invention is illustrated in theattached' Figure 3. This drawing likewise includes a partial showing 'of' theheat exchange and fractionatingequiprnent of Figure lywith similar parts similarly numbered and adifierent monifolding system. In this modification .a portion of the high pressure nitrogen "availablexwithin exchanger 6'! at the top of thehigh pressure section 65 of fractionating tower-60 is'withdrawn through line-2 6l. A portion of'the high pressure nitrogen in this" stream is branched ofi and fed through line-243m lines "44-and45, at arate' controlled by-'-valve"245,-to chill the "by-'pass'air stream inthe exchangers-35 and'3'l.
In this case, chilledand purified airproduced in the by-pass exchanger system is withdrawn through line -257 and combined with *the'main cold air stream w, derived from themain'air regenerators l0 and I2 of Figure 1. The total combined air stream thus prdouced iscooled 'further by exchangers 82 and 83'and passed't'hroug'h line 241 into the bottom of the high "pressure section '65 of tower -60.
The high pressure nitrogen stream 246 is warmed in the same manner as N2 stream 146 in Figure 2 or air stream-46 in Figure 1, bypheat exchange with the by-pass air stream in "condensers 35 and 31." Here, however; it iscombined with and pre warmsthe remaining portion ofthe cold high-pressure'nitrogen from line 261, .in'line 256. The prewarmed nitrogen stream'in'line255, work expanded in expander 259, is rechil'led thereby and passes through line 2Bl to"line 19' leaving the top of the low pressure'section 63 of i the fractionating' tower. Thecooling effect of the workexpansion step is thus availablefor heat exchange-in exchangers '11 and 8i,- in sub' stantially the same manner as in the modification shown in Figure 1.
While the foregoing description has referred to the principal air chilling means as being of the alternaitng regenerative type, they may equally suitably be of the alternating recuperative type. The invention may be applied in a generally analogous manner to the separation of other low boiling gas mixtures into two components of different boiling point. The lower boiling component then takes the place of N2 while the higher boiling component takes that of oxygen. Other modifications within the spirit of the invention may appear to those skilled in the art.
The above description and exemplary operations have served to illustrate specific embodiments of the invention but are not intended to be limiting in scope.
What is claimed is:
1. The method of separating gas mixtures by liquefaction and fractionation which comprises charging the major proportion of a gas mixture to be separated at a super-atmospheric pressure to chilling and purification means to produce cold clean gas, chilling and purifying a minor proportion of said gas mixture in equipment separate from said means at substantially said super-atmospheric pressure so as to cool said minor proportion and remove at least the major proportion of its solidifying constituents, said separate equipment comprising heat exchange means operating by the recuperative principle in chilling cycles and cycles serving the evaporation of solidified gas mixture constituents deposited in said recuperative means, passing a minor proportion of said first named cold clean gas through said recuperative means during their chilling cycle to warm said minor proportion of cold clean gas, passing a minor proportion of said clean gas so warmed through said recuperative means during said cleaning cycle to remove said deposits, mixing the remaining portion of said warmed clean gas with a second minor proportion of said first named cold clean gas, subjecting the mixture so obtained to work expansion to provide refrigeration and utilizing said refrigeration in said process.
2. The process of claim 1 in which said firstnamed minor proportion is withdrawn from said recuperative means at a temperature closely approaching that of said first-mentioned cold clean gas and admixed with said remaining portion of said warmed clean gas prior to said work expansion.
3. The process of claim 1 in which said minor proportion of said warmed clean gas is first chilled by passage through said recuperative means from the warm end to the cold end during the cleaning cycle, employing a flow path free of deposited vaporizable impurities and is then reversed and passed through said recuperative means from the cold end to the warm end through a flow path initially containing deposited vaporizable impurities.
4. The process of claim 3 in which external heat is added to said minorproportion of said warmed clean gas after chilling and before its reversal and reintroduction into the said recuperative means.
5. The process of claim 3 in which a small stream is branched off said minor proportion of said warmed clean gas and by-passed around said recuperative means, and said by-passed stream is then added to the chilled portion of said warmed clean gas before its reversal and reintroduction into the said recuperative means.
6. The process of claim 1 in which said gas mixture is air and said chilling and purification means are cooled by passing therethrough separate streams of cold product nitrogen and oxygen gases.
7. The process of claim 6 in which said separate streams carry a total quantity of gas larger than that of said major proportion of air.
8. The method of separating a gas mixture by liquefaction and fractionation which comprises charging the major portion of the gas mixture at a superatmospheric pressure to chillingand purification means to produce a first stream of cold clean gas by means of heat exchange with separate streams of cold clean gas representing separated product constituents the total quantity of which is larger than the quantity of said major portion of the gas mixture, chilling and purifying the remaining minor portion of said gas mixture at substantially said superatmospheric pressure in equipment separate from said means so as to 0001 said minor portion and remove at least the major part of its solidifying constituents, said separate equipment comprising heat exchange means operating by the recuperative principle in chilling cycles and cycles serving the evaporation of solidified gas constituents deposited therein, passing through said recuperative means during their chilling cycle a relatively small amount of a second clean gas stream derived from one of said streams of cold clean gas to warm said second clean gas stream, passing a minor portion of said second clean gas so warmed through said recuperative means during their cleaning cycle to remove the deposits therefrom, transferring heat absorbed from said first named minor portion of the gas mixture to a third cold clean gas stream derived from one of said streams of cold clean gas maintained at superatmospheric pressure, subjecting the warmed gas in the last named stream to work-expansion to provide refrigeration and utilizing said refrigeration in said process.
9. The method of claim 8 in which said second cold clean gas stream is a minor portion of said first stream of cold clean gas, said third cold clean gas stream is a separate minor portion of said first cold clean gas stream, and said heat transfer is efiected by adding the remaining warmed portion of said second clean gas stream directly to said third stream prior to said work expansion.
10. The method of claim 9 in which said gas mixture is air, said second cold clean gas stream is a chilled portion of said air and said third cold clean gas stream is another chilled portion of said air.
11. The method of claim 8 in which said second cold clean gas stream is a portion of a coldseparated main gas constituent, said third cold clean gas stream is a chilled portion of said gas mixture, and said heat transfer is effected by the indirect exchange of heat between said third stream andat least part of the warmed portion of said second stream.
12. The method of claim 11 in which said gas mixture is air, said second cold clean gas stream is a portion of a cold separated main constituent of air and said third cold clean gas stream is a chilled portion of said air.
13. The method of claim 8 in which said sec- 0nd cold clean gas stream is a portion of a cold separated main gas constituent, said third cold clean gas stream is another portion of a cold separated main gas constituent, and said heat REFERENCES CITED The following references are of record in the file of this patent:
Claims (1)
1. THE METHOD OF SEPARATING GAS MIXTURES BY LIQUEFACTION AND FRACTIONATION WHICH COMPRISES CHARGING THE MAJOR PROPORTION OF A GAS MIXTURE TO BE SEPARATED AT A SUPER-ATMOSPHERIC PRESSURE TO CHILLING AND PURIFICATION MEANS TO PRODUCE COLD CLEAN GAS, CHILLING AND PURIFYING A MINOR PROPORTION OF SAID GAS MIXTURE IN EQUIPMENT SEPARATE FROM SAID MEANS AT SUBSTANTIALLY SAID SUPER-ATMOSPHERIC PRESSURE SO AS TO COOL SAID MINOR PROPORTION AND REMOVE AT LEAST THE MAJOR PROPORTION OF ITS SOLIDIFYING CONSTITUENTS, SAID SEPARATE EQUIPMENT COMPRISING HEAT EXCHARGE MEANS OPERATING BY THE RECUPERATIVE PRINCIPLE IN CHILLING CYCLES AND CYCLES SERVING THE EVAPORATION OF SOLIDIFIED GAS MIXTURE CONSTITUENTS DEPOSITED IN SAID RECUPERATIVE MEANS, PASSING A MINOR PROPORTION OF SAID FIRST NAMED COLD CLEAN GAS THROUGH SAID RECUPERATIVE MEANS DURING THEIR CHILLING CYCLE TO WARM SAID MINOR PROPORTION OF COLD CLEAN GAS, PASSING A MINOR PROPORTION OF SAID CLEAN GAS SO WARMED THROUGH SAID RECUPERATIVE MEANS DURING SAID CLEANING CYCLE TO REMOVE SAID DEPOSITS, MIXING THE REMAINING PORTION OF SAID WARMED CLEAN GAS WITH A SECOND MINOR PROPORTION OF SAID FIRST NAMED COLD CLEAN GAS, SUBJECTING THE MIXTURE SO OBTAINED TO WORK EXPANSION TO PROVIDE REFRIGERATION AND UTILIZING SAID REFRIGERATION IN SAID PROCESS.
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US (1) | US2622416A (en) |
Cited By (12)
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---|---|---|---|---|
US2802349A (en) * | 1951-08-25 | 1957-08-13 | Kellogg M W Co | Removing impurities from a gas liquefaction system with aid of extraneous gas stream |
US2917902A (en) * | 1954-08-06 | 1959-12-22 | Commissariat Energie Atomique | Gas purification process |
US2918801A (en) * | 1955-10-10 | 1959-12-29 | Union Carbide Corp | Process and apparatus for separating gas mixtures |
US2955434A (en) * | 1956-10-15 | 1960-10-11 | Air Prod Inc | Method and apparatus for fractionating gaseous mixtures |
US2968160A (en) * | 1956-04-09 | 1961-01-17 | Air Prod Inc | Method and apparatus for separating gaseous mixtures including high boiling point impurities |
US3036439A (en) * | 1954-10-01 | 1962-05-29 | Stamicarbon | Purification of a gas by removing one or more admixed impurities from it by condensing the impurity or impurities to the solid state |
US3066494A (en) * | 1958-05-26 | 1962-12-04 | Union Carbide Corp | Process of and apparatus for low-temperature separation of air |
US3126265A (en) * | 1964-03-24 | Process and apparatus for separating | ||
US3196621A (en) * | 1959-11-17 | 1965-07-27 | Linde Eismasch Ag | Method of separating air by low temperature rectification |
US3254495A (en) * | 1963-06-10 | 1966-06-07 | Fluor Corp | Process for the liquefaction of natural gas |
US3264831A (en) * | 1962-01-12 | 1966-08-09 | Linde Ag | Method and apparatus for the separation of gas mixtures |
TWI575348B (en) * | 2014-12-25 | 2017-03-21 | 東芝股份有限公司 | Air supply system |
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US2334632A (en) * | 1937-08-28 | 1943-11-16 | Koehler Franz | Recovery of nitrogen and oxygen |
US2433604A (en) * | 1945-10-30 | 1947-12-30 | Air Reduction | Separation of the constituents of gaseous mixtures |
US2496380A (en) * | 1946-04-18 | 1950-02-07 | Elliott Co | Gas purifying method and apparatus |
US2504051A (en) * | 1947-04-30 | 1950-04-11 | Hydrocarbon Research Inc | Process for producing oxygen by liquefaction of air in which a portion of the air is expanded to supply refrigeration without loss of oxygen content of the air |
US2513306A (en) * | 1947-11-01 | 1950-07-04 | Hydrocarbon Research Inc | Process for producing oxygen by the liquefaction and rectification of air |
US2526996A (en) * | 1947-02-21 | 1950-10-24 | Elliott Co | Method and apparatus for separating mixed gases |
US2579498A (en) * | 1946-12-21 | 1951-12-25 | Hydrocarbon Research Inc | Process for producing oxygen |
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US2334632A (en) * | 1937-08-28 | 1943-11-16 | Koehler Franz | Recovery of nitrogen and oxygen |
US2433604A (en) * | 1945-10-30 | 1947-12-30 | Air Reduction | Separation of the constituents of gaseous mixtures |
US2496380A (en) * | 1946-04-18 | 1950-02-07 | Elliott Co | Gas purifying method and apparatus |
US2579498A (en) * | 1946-12-21 | 1951-12-25 | Hydrocarbon Research Inc | Process for producing oxygen |
US2526996A (en) * | 1947-02-21 | 1950-10-24 | Elliott Co | Method and apparatus for separating mixed gases |
US2504051A (en) * | 1947-04-30 | 1950-04-11 | Hydrocarbon Research Inc | Process for producing oxygen by liquefaction of air in which a portion of the air is expanded to supply refrigeration without loss of oxygen content of the air |
US2513306A (en) * | 1947-11-01 | 1950-07-04 | Hydrocarbon Research Inc | Process for producing oxygen by the liquefaction and rectification of air |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3126265A (en) * | 1964-03-24 | Process and apparatus for separating | ||
US2802349A (en) * | 1951-08-25 | 1957-08-13 | Kellogg M W Co | Removing impurities from a gas liquefaction system with aid of extraneous gas stream |
US2917902A (en) * | 1954-08-06 | 1959-12-22 | Commissariat Energie Atomique | Gas purification process |
US3036439A (en) * | 1954-10-01 | 1962-05-29 | Stamicarbon | Purification of a gas by removing one or more admixed impurities from it by condensing the impurity or impurities to the solid state |
US2918801A (en) * | 1955-10-10 | 1959-12-29 | Union Carbide Corp | Process and apparatus for separating gas mixtures |
US2968160A (en) * | 1956-04-09 | 1961-01-17 | Air Prod Inc | Method and apparatus for separating gaseous mixtures including high boiling point impurities |
US2955434A (en) * | 1956-10-15 | 1960-10-11 | Air Prod Inc | Method and apparatus for fractionating gaseous mixtures |
US3066494A (en) * | 1958-05-26 | 1962-12-04 | Union Carbide Corp | Process of and apparatus for low-temperature separation of air |
US3196621A (en) * | 1959-11-17 | 1965-07-27 | Linde Eismasch Ag | Method of separating air by low temperature rectification |
US3264831A (en) * | 1962-01-12 | 1966-08-09 | Linde Ag | Method and apparatus for the separation of gas mixtures |
US3254495A (en) * | 1963-06-10 | 1966-06-07 | Fluor Corp | Process for the liquefaction of natural gas |
TWI575348B (en) * | 2014-12-25 | 2017-03-21 | 東芝股份有限公司 | Air supply system |
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